@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP315114.RAhkHjm94ANl4OMCkCfQtDa0KNKWGDqmVCJEbMHufoH5M
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP315114.RAhkHjm94ANl4OMCkCfQtDa0KNKWGDqmVCJEbMHufoH5M130_head
{
this:
np:hasAssertion
dgn-np:NP315114.RAhkHjm94ANl4OMCkCfQtDa0KNKWGDqmVCJEbMHufoH5M130_assertion
;
np:hasProvenance
dgn-np:NP315114.RAhkHjm94ANl4OMCkCfQtDa0KNKWGDqmVCJEbMHufoH5M130_provenance
;
np:hasPublicationInfo
dgn-np:NP315114.RAhkHjm94ANl4OMCkCfQtDa0KNKWGDqmVCJEbMHufoH5M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP315114.RAhkHjm94ANl4OMCkCfQtDa0KNKWGDqmVCJEbMHufoH5M130_assertion
a
np:Assertion
.
dgn-np:NP315114.RAhkHjm94ANl4OMCkCfQtDa0KNKWGDqmVCJEbMHufoH5M130_provenance
a
np:Provenance
.
dgn-np:NP315114.RAhkHjm94ANl4OMCkCfQtDa0KNKWGDqmVCJEbMHufoH5M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP315114.RAhkHjm94ANl4OMCkCfQtDa0KNKWGDqmVCJEbMHufoH5M130_assertion
{
miriam-gene:5444
a
ncit:C16612
.
lld:C0149931
a
ncit:C7057
.
dgn-gda:DGNb0dd60ad2234e93fe2bb3d27fc6a692b
sio:SIO_000628
miriam-gene:5444
,
lld:C0149931
;
a
sio:SIO_001121
.
}
dgn-np:NP315114.RAhkHjm94ANl4OMCkCfQtDa0KNKWGDqmVCJEbMHufoH5M130_provenance
{
dgn-np:NP315114.RAhkHjm94ANl4OMCkCfQtDa0KNKWGDqmVCJEbMHufoH5M130_assertion
dcterms:description
"[The frequencies of the PON1 genotypes and PON1 allelic variants did not differ significantly between patients with migraine and controls, and were unrelated with gender, family history of migraine, and presence or absence of aura.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:20407783
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP315114.RAhkHjm94ANl4OMCkCfQtDa0KNKWGDqmVCJEbMHufoH5M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:00+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}